BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 28695818)

  • 1. Progress in Molecular Genetic Study of Mitochondrial Cardiomyopathy.
    Zhuge R; Zhou R; Ni X
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2017 Jun; 39(3):438-444. PubMed ID: 28695818
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.
    Meyers DE; Basha HI; Koenig MK
    Tex Heart Inst J; 2013; 40(4):385-94. PubMed ID: 24082366
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neonatal cardiomyopathies and metabolic crises due to oxidative phosphorylation defects.
    Schiff M; Ogier de Baulny H; Lombès A
    Semin Fetal Neonatal Med; 2011 Aug; 16(4):216-21. PubMed ID: 21606011
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial Genome Variants as a Cause of Mitochondrial Cardiomyopathy.
    Campbell T; Slone J; Huang T
    Cells; 2022 Sep; 11(18):. PubMed ID: 36139411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cardiomyopathies Due to Left Ventricular Noncompaction, Mitochondrial and Storage Diseases, and Inborn Errors of Metabolism.
    Towbin JA; Jefferies JL
    Circ Res; 2017 Sep; 121(7):838-854. PubMed ID: 28912186
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Electron transport chain defects in heart failure.
    Casademont J; Miró O
    Heart Fail Rev; 2002 Apr; 7(2):131-9. PubMed ID: 11988637
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Review: Metabolic cardiomyopathy and conduction system defects in children.
    Gilbert-Barness E
    Ann Clin Lab Sci; 2004; 34(1):15-34. PubMed ID: 15038665
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Clinical, biochemical and genetic analysis of the mitochondrial disorders presenting with cardiac damage].
    Ma YY; Wu TF; Liu YP; Wang Q; Li XY; Ding Y; Song JQ; Yang YL
    Zhonghua Er Ke Za Zhi; 2013 Dec; 51(12):909-14. PubMed ID: 24495761
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparison of electron microscopic findings and clinical presentation in three patients with mitochondrial cardiomyopathy caused by the mitochondrial DNA mutation m.3243A > G.
    Saku T; Takashio S; Tsuruta Y; Otsuka Y; Takae M; Kiyama T; Yamamoto E; Kaikita K; Hotta T; Matsumoto S; Kang D; Tsujita K; Komohara Y
    Med Mol Morphol; 2021 Jun; 54(2):181-186. PubMed ID: 33113037
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Exome sequencing identifies mitochondrial alanyl-tRNA synthetase mutations in infantile mitochondrial cardiomyopathy.
    Götz A; Tyynismaa H; Euro L; Ellonen P; Hyötyläinen T; Ojala T; Hämäläinen RH; Tommiska J; Raivio T; Oresic M; Karikoski R; Tammela O; Simola KO; Paetau A; Tyni T; Suomalainen A
    Am J Hum Genet; 2011 May; 88(5):635-42. PubMed ID: 21549344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Do mitochondria contribute to left ventricular non-compaction cardiomyopathy? New findings from myocardium of patients with left ventricular non-compaction cardiomyopathy.
    Liu S; Bai Y; Huang J; Zhao H; Zhang X; Hu S; Wei Y
    Mol Genet Metab; 2013 May; 109(1):100-6. PubMed ID: 23465694
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial Cardiomyopathies.
    El-Hattab AW; Scaglia F
    Front Cardiovasc Med; 2016; 3():25. PubMed ID: 27504452
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Advances in Diagnosis and Management of Mitochondrial Cardiomyopathy.
    Zhuge R; Zhou R; Ni X
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2017 Apr; 39(2):290-295. PubMed ID: 28483032
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options.
    Lioncino M; Monda E; Caiazza M; Fusco A; Cirillo A; Dongiglio F; Simonelli V; Sampaolo S; Ruggiero L; Scarano G; Pota V; Frisso G; Mazzaccara C; D'Amati G; Nigro G; Russo MG; Wahbi K; Limongelli G
    Heart Fail Clin; 2022 Jan; 18(1):51-60. PubMed ID: 34776083
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel rat model of multiple mitochondrial dysfunction syndromes (MMDS) complicated with cardiomyopathy.
    Ling Y; Ma J; Qi X; Zhang X; Kong Q; Guan F; Dong W; Chen W; Gao S; Gao X; Pan S; Ma Y; Lu D; Zhang L
    Animal Model Exp Med; 2021 Dec; 4(4):381-390. PubMed ID: 34977489
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondria and heart disease.
    DiMauro S; Hirano M
    Curr Opin Cardiol; 1998 May; 13(3):190-7. PubMed ID: 9649942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.
    Limongelli G; Masarone D; D'Alessandro R; Elliott PM
    Future Cardiol; 2012 Jan; 8(1):71-88. PubMed ID: 22185447
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A switch in metabolism precedes increased mitochondrial biogenesis in respiratory chain-deficient mouse hearts.
    Hansson A; Hance N; Dufour E; Rantanen A; Hultenby K; Clayton DA; Wibom R; Larsson NG
    Proc Natl Acad Sci U S A; 2004 Mar; 101(9):3136-41. PubMed ID: 14978272
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Severe obstructive hypertrophic cardiomyopathy occurring secondary to mitochondrial disease.
    Izgi C; Cevik C; Bakal RB; Ozkan M
    Turk Kardiyol Dern Ars; 2009 Jul; 37(5):332-6. PubMed ID: 19875907
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Clinical spectrum, morbidity, and mortality in 113 pediatric patients with mitochondrial disease.
    Scaglia F; Towbin JA; Craigen WJ; Belmont JW; Smith EO; Neish SR; Ware SM; Hunter JV; Fernbach SD; Vladutiu GD; Wong LJ; Vogel H
    Pediatrics; 2004 Oct; 114(4):925-31. PubMed ID: 15466086
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.